Canonical Allele Identifier: CA375730216
Gene: GRIN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137167523G>A , CM000671.2:g.137167523G>A GRCh38
NC_000009.11:g.140061975G>A , CM000671.1:g.140061975G>A GRCh37
NC_000009.10:g.139181796G>A NCBI36
NG_011507.1:g.33367G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000371553.8:c.2764-251G>A ENSP00000360608.3:n.2764-251G>A
ENST00000371560.5:c.2653-251G>A ENSP00000360615.3:n.2653-251G>A
ENST00000371561.8:c.2813G>A MANE Select ENSP00000360616.3:p.Ser938Asn
ENST00000371546.8:c.2876G>A ENSP00000360601.4:p.Ser959Asn
ENST00000371550.8:c.2702G>A ENSP00000360605.4:p.Ser901Asn
ENST00000371553.7:c.2764-251G>A ENSP00000360608.3:n.2764-251G>A
ENST00000371555.8:c.2765G>A ENSP00000360610.4:p.Ser922Asn
ENST00000371559.8:c.2590-251G>A ENSP00000360614.4:n.2590-251G>A
ENST00000371560.4:c.2653-251G>A ENSP00000360615.3:n.2653-251G>A
ENST00000371561.7:c.2813G>A ENSP00000360616.3:p.Ser938Asn
ENST00000473811.1:n.293G>A
NM_000832.6:c.2590-251G>A NP_000823.4:n.2590-251G>A
NM_001185090.1:c.2764-251G>A NP_001172019.1:n.2764-251G>A
NM_001185091.1:c.2653-251G>A NP_001172020.1:n.2653-251G>A
NM_007327.3:c.2813G>A NP_015566.1:p.Ser938Asn
NM_021569.3:c.2702G>A NP_067544.1:p.Ser901Asn
XM_005266071.2:c.2701-251G>A XP_005266128.1:n.2701-251G>A
XM_005266072.2:c.2765G>A XP_005266129.1:p.Ser922Asn
XM_005266073.3:c.2876G>A XP_005266130.1:p.Ser959Asn
XM_005266071.3:c.2701-251G>A XP_005266128.1:n.2701-251G>A
XM_005266072.3:c.2765G>A XP_005266129.1:p.Ser922Asn
XM_005266073.4:c.2876G>A XP_005266130.1:p.Ser959Asn
NM_007327.4:c.2813G>A MANE Select NP_015566.1:p.Ser938Asn
NM_000832.7:c.2590-251G>A NP_000823.4:n.2590-251G>A
NM_001185090.2:c.2764-251G>A NP_001172019.1:n.2764-251G>A
NM_001185091.2:c.2653-251G>A NP_001172020.1:n.2653-251G>A
NM_021569.4:c.2702G>A NP_067544.1:p.Ser901Asn